Canonical Allele Identifier: CA2499923405

Gene: EVC CRMP1

Genomic Alleles

HGVS	Genome Assembly
NC_000004.12:g.5808502_5808503insGCCCTGGAACCCTT , CM000666.2:g.5808502_5808503insGCCCTGGAACCCTT	GRCh38
NC_000004.11:g.5810229_5810230insGCCCTGGAACCCTT , CM000666.1:g.5810229_5810230insGCCCTGGAACCCTT	GRCh37
NC_000004.10:g.5861130_5861131insGCCCTGGAACCCTT	NCBI36
NG_008843.1:g.102306_102307insGCCCTGGAACCCTT

Transcript Alleles

HGVS	Amino-acid Change
ENST00000264956.11:c.2688+175_2688+176insGCCCTGGAACCCTT (EVC) MANE Select	ENSP00000264956.6:n.2688+175_2688+176insGCCCTGGAACCCTT
ENST00000264956.10:c.2688+175_2688+176insGCCCTGGAACCCTT (EVC)	ENSP00000264956.6:n.2688+175_2688+176insGCCCTGGAACCCTT
ENST00000506216.5:n.1647+16991_1647+16992insAAGGGTTCCAGGGC (CRMP1)
NM_001306090.1:c.2688+175_2688+176insGCCCTGGAACCCTT (EVC)	NP_001293019.1:n.2688+175_2688+176insGCCCTGGAACCCTT
NM_153717.2:c.2688+175_2688+176insGCCCTGGAACCCTT (EVC)	NP_714928.1:n.2688+175_2688+176insGCCCTGGAACCCTT
XM_006713865.2:c.2688+175_2688+176insGCCCTGGAACCCTT (EVC)	XP_006713928.1:n.2688+175_2688+176insGCCCTGGAACCCTT
XM_006713866.2:c.2688+175_2688+176insGCCCTGGAACCCTT (EVC)	XP_006713929.1:n.2688+175_2688+176insGCCCTGGAACCCTT
XR_427473.2:n.2878+175_2878+176insGCCCTGGAACCCTT (EVC)
XR_427475.2:n.2878+175_2878+176insGCCCTGGAACCCTT (EVC)
XR_427476.2:n.2878+175_2878+176insGCCCTGGAACCCTT (EVC)
XR_924920.1:n.2878+175_2878+176insGCCCTGGAACCCTT (EVC)
XR_924921.1:n.2878+175_2878+176insGCCCTGGAACCCTT (EVC)
XR_924922.1:n.2878+175_2878+176insGCCCTGGAACCCTT (EVC)
XR_924923.1:n.2878+175_2878+176insGCCCTGGAACCCTT (EVC)
XR_924924.1:n.2878+175_2878+176insGCCCTGGAACCCTT (EVC)
XR_924925.1:n.2878+175_2878+176insGCCCTGGAACCCTT (EVC)
XR_924926.1:n.2878+175_2878+176insGCCCTGGAACCCTT (EVC)
XR_924927.1:n.2878+175_2878+176insGCCCTGGAACCCTT (EVC)
XM_006713865.3:c.2688+175_2688+176insGCCCTGGAACCCTT (EVC)	XP_006713928.1:n.2688+175_2688+176insGCCCTGGAACCCTT
XM_006713866.3:c.2688+175_2688+176insGCCCTGGAACCCTT (EVC)	XP_006713929.1:n.2688+175_2688+176insGCCCTGGAACCCTT
XR_001741164.1:n.2868+175_2868+176insGCCCTGGAACCCTT (EVC)
XR_001741165.1:n.2868+175_2868+176insGCCCTGGAACCCTT (EVC)
XR_001741166.1:n.2868+175_2868+176insGCCCTGGAACCCTT (EVC)
XR_001741167.1:n.2868+175_2868+176insGCCCTGGAACCCTT (EVC)
XR_001741168.1:n.2868+175_2868+176insGCCCTGGAACCCTT (EVC)
XR_001741169.2:n.2732+175_2732+176insGCCCTGGAACCCTT (EVC)
XR_001741170.1:n.2953+175_2953+176insGCCCTGGAACCCTT (EVC)
XR_001741171.1:n.2173+175_2173+176insGCCCTGGAACCCTT (EVC)
XR_427473.3:n.2868+175_2868+176insGCCCTGGAACCCTT (EVC)
XR_427475.3:n.2868+175_2868+176insGCCCTGGAACCCTT (EVC)
XR_427476.3:n.2868+175_2868+176insGCCCTGGAACCCTT (EVC)
XR_924920.2:n.2868+175_2868+176insGCCCTGGAACCCTT (EVC)
XR_924921.2:n.2868+175_2868+176insGCCCTGGAACCCTT (EVC)
XR_924922.2:n.2868+175_2868+176insGCCCTGGAACCCTT (EVC)
XR_924924.2:n.2868+175_2868+176insGCCCTGGAACCCTT (EVC)
XR_924925.2:n.2868+175_2868+176insGCCCTGGAACCCTT (EVC)
XR_924926.2:n.2868+175_2868+176insGCCCTGGAACCCTT (EVC)
NM_153717.3:c.2688+175_2688+176insGCCCTGGAACCCTT (EVC) MANE Select	NP_714928.1:n.2688+175_2688+176insGCCCTGGAACCCTT
NM_001306090.2:c.2688+175_2688+176insGCCCTGGAACCCTT (EVC)	NP_001293019.1:n.2688+175_2688+176insGCCCTGGAACCCTT